CAS 38753-75-2
:Pregn-4-ene-21-carboxylic acid, 17-hydroxy-7-(methylsulfinyl)-3-oxo-, γ-lactone, (7α,17α)-
Description:
Pregn-4-ene-21-carboxylic acid, 17-hydroxy-7-(methylsulfinyl)-3-oxo-, γ-lactone, (7α,17α)-, commonly referred to by its CAS number 38753-75-2, is a synthetic steroid compound characterized by its complex structure, which includes a pregnane backbone. This compound features a carboxylic acid functional group, a hydroxyl group, and a methylsulfinyl moiety, contributing to its unique chemical properties. The presence of the γ-lactone ring indicates that it can exhibit specific reactivity patterns typical of lactones, such as ring-opening reactions under certain conditions. Its stereochemistry, denoted by the (7α,17α)- configuration, suggests specific spatial arrangements of its substituents, which can influence its biological activity and interactions with receptors. This compound may be of interest in pharmaceutical research, particularly in the development of therapeutic agents due to its steroidal nature. However, detailed studies on its pharmacokinetics, mechanisms of action, and potential applications would be necessary to fully understand its utility in medicinal chemistry.
Formula:C23H32O4S
InChI:InChI=1/C23H32O4S/c1-21-8-4-15(24)12-14(21)13-18(28(3)26)20-16(21)5-9-22(2)17(20)6-10-23(22)11-7-19(25)27-23/h12,16-18,20H,4-11,13H2,1-3H3/t16-,17-,18+,20+,21-,22-,23+,28?/m0/s1
InChI key:InChIKey=ADVFYBFTUKGFGC-FLWPULIFSA-N
SMILES:C[C@@]12[C@]3(CC[C@]1([C@]4([C@](CC2)([C@]5(C)C(C[C@H]4S(C)=O)=CC(=O)CC5)[H])[H])[H])OC(=O)CC3
Synonyms:- Pregn-4-ene-21-carboxylic acid, 17-hydroxy-7-(methylsulfinyl)-3-oxo-, γ-lactone, (7α,17α)-
- Spiro[17H-cyclopenta[a]phenanthrene-17,2′(5′H)-furan], pregn-4-ene-21-carboxylic acid deriv.
- 3-(3-Oxo-7α-methylsulfinyl-17β-hydroxy-4-androsten-17α-yl)propionic acid γ-lactone
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